RecallRadar

FDA Device recall Z-2626-2015

SHOULDER ARTHROSCOPY PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, sutu…

On 2015-09-09 the FDA classified a Class II recall of SHOULDER ARTHROSCOPY PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, sutu… by Customed, citing recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2626-2015
ClassificationClass II
Statusterminated
Initiated2015-07-10
Published2015-09-09
Last updated2026-09-13 11:53 UTC
CompanyCustomed
DistributionPR

Product

SHOULDER ARTHROSCOPY PACK 3/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .

Reason

Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.

Identifiers

code_info
Code:9002193 Lots: 141015703 exp. 11/30/15 141216299 exp. 12/31/15 150116522 exp. 12/31/15 150217450 exp. 2/28/16…Code:9002193 Lots: 141015703 exp. 11/30/15 141216299 exp. 12/31/15 150116522 exp. 12/31/15 150217450 exp. 2/28/16 150217451 exp. 2/28/16 150317723 exp. 3/31/16 150317724 exp. 4/30/16 150418349 exp. 4/30/16 150418350 exp. 4/30/16 150619192 exp. 6/30/16

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2626-2015%22

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